tyrosine has been researched along with Abnormalities, Teeth in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cai, T; Dong, M; Duan, X; Gao, S; He, L; Hu, K; Li, Q; Mao, T; Shi, S; Wang, L; Xia, D; Xue, Y | 1 |
| Blau, N; Dill, P; Jakobs, C; Schneider, J; Tekin, M; Thöny, B; Trachsel, D; Weber, P | 1 |
| Dingerdissen, H; Karagiannis, K; Mazumder, R; Motwani, M; Simonyan, V | 1 |
3 other study(ies) available for tyrosine and Abnormalities, Teeth
| Article | Year |
|---|---|
Dental Abnormalities Caused by Novel Compound Heterozygous CTSK Mutations.
Topics: Adenine; Adult; Alleles; Alveolar Process; Amino Acid Sequence; Animals; Cathepsin K; Chlorocebus aethiops; Codon, Terminator; Conserved Sequence; COS Cells; Cysteine; Dental Cementum; Guanine; Heterozygote; Humans; Male; Models, Genetic; Mutation, Missense; Pedigree; Phenol; Pycnodysostosis; Radiography, Panoramic; Tooth Abnormalities; Tryptophan; Tyrosine; X-Ray Microtomography | 2015 |
Pyridoxal phosphate-responsive seizures in a patient with cerebral folate deficiency (CFD) and congenital deafness with labyrinthine aplasia, microtia and microdontia (LAMM).
Topics: Base Sequence; Child; Codon, Nonsense; Congenital Abnormalities; Congenital Microtia; Dihydroxyphenylalanine; DNA Primers; Ear; Ear, Inner; Electroencephalography; Epilepsy; Fibroblast Growth Factor 3; Folate Receptor 1; Folic Acid Deficiency; Humans; Levodopa; Male; Molecular Sequence Data; Pyridoxal Phosphate; Radiography; Sequence Analysis, DNA; Skull; Syndrome; Tooth Abnormalities; Tyrosine | 2011 |
Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins.
Topics: Abnormalities, Multiple; Amino Acid Substitution; Arginine; Aspartic Acid; Carbohydrate Metabolism; Catalytic Domain; Cluster Analysis; Enzyme Activation; Genetic Variation; Genome, Human; Glycogen Storage Disease; Hearing Loss; Histidine; Humans; Lacrimal Apparatus Diseases; Metabolomics; Molecular Sequence Annotation; Phenylalanine; Polymorphism, Single Nucleotide; Proteome; Proteomics; Structure-Activity Relationship; Syndactyly; Tooth Abnormalities; Tyrosine | 2013 |